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NCT00212927 Clinical Trial

Continuity of Care and Outcomes After Discharge From Hospital

Patient Safety Clinical Trial

Official title:
The Association of Provider Continuity and Information Continuity With Patient Outcomes After Discharge From Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00212927
Other study ID # carl001
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated August 31, 2015
Start date October 2002
Est. completion date December 2006

Study information
Verified date July 2007
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Observational

Clinical Trial Summary

1. INTRODUCTION: Continuity of care (COC) occurs when separate elements of patient care are connected. COC is made up primarily of Continuity of Provider (COP) and Continuity of Information (COI). Many authorities believe that COC is essential to high-quality care. Previous studies have shown poor COC in varied populations. Many studies have shown that increased COC has been associated with improved intermediate outcomes. However, no study has definitively determined whether COC or either of its components is associated with important outcomes. The Ontario-Outcomes After the Hospitalization (Ontario-OAtH) study will enroll 5900 adults who are discharged to the community from medical and surgical services from 13 teaching and community hospitals in 5 regions across Ontario. Patients will be followed for 6 months to record details about all interactions with the health care system. This information will give us a detailed measure of both provider and information continuity for all patients over time. The Ontario-OAtH study will have the power to precisely determine whether COC is associated with time to urgent readmission or death after hospital discharge. Since COC is potentially modifiable, the Ontario-OAtH study will give us essential information required for designing interventions to improve outcomes for patients after they are discharged from hospital.

Description:

See above

Recruitment information / eligibility
Status Completed
Enrollment 5900
Est. completion date December 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- discharged to the community from medical and surgical services

Exclusion Criteria:

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Canada Ottawa Health Research Institute Ottawa Ontario

Sponsors (1)
Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

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